Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g01970 | A06 | 1199107 | C | T | missense_variant | MODERATE | c.503G>A|p.Gly168Asp |
S261 |
2 | BAA06g01970 | A06 | 1203087 | G | A | upstream_gene_variant | MODIFIER | c.-3238C>T| |
S257 |
3 | BAA06g01970 | A06 | 1203969 | G | A | upstream_gene_variant | MODIFIER | c.-4120C>T| |
S166 |
4 | BAA06g01970 | A06 | 1204845 | C | T | upstream_gene_variant | MODIFIER | c.-4996G>A| |
S270 |